Package: ExomeDepth
Type: Package
Title: Calls Copy Number Variants from Targeted Sequence Data
Version: 1.1.15
Date: 2019-12-23
Encoding: UTF-8
Depends: R (>= 3.4.0)
Imports: Biostrings, IRanges, Rsamtools, GenomicRanges (>= 1.23.0),
        aod, VGAM (>= 0.8.4), methods, GenomicAlignments, dplyr,
        magrittr
Suggests: knitr
VignetteBuilder: knitr
Authors@R: c(person("Vincent", "Plagnol", role = c("aut", "cre"), email = "v.plagnol@ucl.ac.uk"))
Maintainer: Vincent Plagnol  <v.plagnol@ucl.ac.uk>
Description: Calls copy number variants (CNVs) from targeted sequence data, typically exome sequencing experiments designed to identify the genetic basis of Mendelian disorders.
License: GPL-3
RoxygenNote: 7.0.2
NeedsCompilation: yes
Packaged: 2019-12-31 20:58:43 UTC; vincent
Author: Vincent Plagnol [aut, cre]
Repository: CRAN
Date/Publication: 2020-01-09 00:50:02 UTC
Built: R 4.1.0; x86_64-w64-mingw32; 2020-08-03 03:44:22 UTC; windows
Archs: i386, x64
